A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779477



Internal ID18831874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51066958..51104019hg38UCSC Ensembl
Innerchr2:51294096..51331157hg19UCSC Ensembl
Innerchr2:51147600..51184661hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3837062
hg1937062
hg1837062
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892204
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779477
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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